| NDC Code | 68071-4966-4 |
|---|
| Package Description | 4 TABLET, FILM COATED in 1 BOTTLE (68071-4966-4) |
|---|
| Product NDC | 68071-4966 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron Hydrochloride |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20070731 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078539 |
|---|
| Manufacturer | NUCARE PHARMACEUTICALS INC |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 8 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|